All recalls
- 2026-02-26CPSCSN Commerce LLC, dba TheKiddoSpaceStore, of Dover, DelawareTheKiddoSpace Recalls Peg Doll Children's Toys Due to Risk of Serious Injury or Death from Choking Hazard; Violate Small Parts Ban
The recalled toys are intended for children under three years old and the toy's peg dolls can block a child's airway, which violate the small parts ban, posing a risk of choking and death to children.
- 2026-02-26CPSCSN Commerce LLC, dba TheKiddoSpaceStore, of Dover, DelawareTheKiddoSpace Recalls LED Soccer Hover Balls Due to Serious Risk of Injury from Burn Hazard; Violates Mandatory Standard for Toys
The surface temperature of the recalled toys' batteries exceeds the allowable limit, which violates the standard for toys, posing a risk of burn injuries.
- 2026-02-26CPSCSN Commerce LLC, dba TheKiddoSpaceStore, of Dover, DelawareTheKiddoSpace Recalls Children's Montessori Egg Puzzle Toys Due to Risk of Serious Injury or Death from Choking Hazard
The recalled toys are intended for children under three years of age and the eggs can block a child's airway, posing a risk of choking and death to children.
- 2026-02-26CPSCSN Commerce LLC, dba TheKiddoSpaceStore, of Dover, DelawareTheKiddoSpace Recalls Children's Flashcard Talking Toys Due to Risk of Injury from Lead and Phthalate Exposure; Violates Federal Lead Content and Phthalates Bans and Standard for Toys
The recalled children's flashcard toy sets contain levels of lead that exceed the federal lead content ban and levels of phthalates that exceed the federal phthalates ban. Lead and phthalates are toxic if ingested by young children and can cause adverse health issues. In addition, the flashcards also violate the mandatory standard for toys because they fail to comply with the short circuit protection requirement for battery-operated toys.
- 2026-02-26CPSCSN Commerce LLC, dba TheKiddoSpaceStore, of Dover, DelawareTheKiddoSpace Recalls Reusable Water Balloons Due to Risk of Injury from Phthalate Exposure; Violate Federal Phthalates Ban
The cord lock on the recalled water ballons' storage bags contain a regulated phthalate, which violate the federal phthalate ban. Phthalates are toxic if ingested by young children and can cause adverse health effects.
- 2026-02-26CPSCSN Commerce LLC, dba TheKiddoSpaceStore, of Dover, DelawareTheKiddoSpace Recalls Children's Fingerpainting Kits Due to Risk of Injury from Hazardous Substances and Phthalate Exposure; Violates Federal Hazardous Substances Act and Phthalates Ban
The recalled children’s fingerpainting kits contain the hazardous substances methanol and ethylene glycol and are intended for children under 12 years of age, which violate the Federal Hazardous Substances Act. The products also contain a regulated phthalate, which violate the federal phthalate ban; phthalates are toxic if ingested by young children and can cause adverse health effects.
- 2026-02-26CPSCSN Commerce LLC, dba TheKiddoSpaceStore, of Dover, DelawareTheKiddoSpace Recalls Children's Handwriting Practice Kits Due to Risk of Injury from Lead Exposure; Violates Federal Lead Content Ban
The pens in the recalled children's handwriting kits contain levels of lead in the nib that exceed the federal lead content ban. Lead is toxic if ingested by young children and can cause adverse health issues.
- 2026-02-26CPSCSN Commerce LLC, dba TheKiddoSpaceStore, of Dover, DelawareTheKiddoSpace Recalls Children's Story Books Due to Choking Hazard
The recalled book's felt parts can detach, posing a choking hazard.
- 2026-02-26CPSCShanghaijinlianwangluokejiyouxiangongsi (Shanghai Jinlian Network Technology Co., Ltd.), dba Grtard, of ChinaGrtard Magnetic Stick Figure Toy Sets Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violates Mandatory Standard for Toys
The magnetic stick figure toy sets violate the mandatory standard for toys because they contain loose magnets, posing an ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other, or other metal objects, and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.
- 2026-02-26CPSCHebei Beihong Kejiyouxiangongsi, dba Bicystar Group Co., Ltd. and Bicystar Store, of ChinaBicystar High Chairs Recalled Due to Risk of Serious Injury or Death from Fall and Entrapment Hazards; Violates Mandatory Standard for High Chairs
The high chairs violate the mandatory standard for high chairs because they were sold without the required attached crotch restraint, posing a deadly fall hazard for children. In addition, a child's head can become trapped between the seat and the side of the high chair, posing a deadly entrapment hazard.
- 2026-02-26CPSCYiwushixiuxiangfushiyouxiangongsi ("Yiwu Xiu Xiang Garment Co., Ltd.") dba Kaiwenshangpin, of ChinaMagnetic Chess Games Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violates Mandatory Standard for Toys; Sold on Amazon by Kaiwenshangpin
The recalled magnetic chess games violate the mandatory standard for toys because they contain loose magnets posing an ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other, or other metal objects, and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.
- 2026-02-26CPSCShenzhenshirongmanshangmaoyouxiangongsi (Shenzhen Shi Ronmang Trading Co., Ltd.) dba Trankerloop, of ChinaTrankerloop Baby Bath Seats Recalled Due to Risk of Serious Injury or Death to Children from Drowning; Violates Mandatory Standard for Infant Bath Seats
The recalled bath seats violate the mandatory standard for infant bath seats because they are unstable and can tip over while in use, posing a risk of serious injury or death due to drowning.
- 2026-02-26CPSCSurreal Brands LLC, of Brooklyn, New YorkSurreal Brands Recalls Children's Tubby Tots Fizzy Flask Bath Magic Bath Foam Sets Due to Impact Hazard
Moisture trapped inside the bath foam set container can cause pressure to build up, allowing pieces to be forcefully ejected when opened, posing an impact hazard.
- 2026-02-26CPSCShenzhen Elephant Outdoor Information Technology Inc. dba Elepdv, of ChinaSomgem Pig and Yomin Toilet Lighters Recalled Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Violates Mandatory Standard for Cigarette Lighters; Sold on Amazon by Elepdv
The recalled pig and toilet lighters violate the mandatory standard for cigarette lighters because they do not have the required child-resistant mechanisms, posing a serious risk of injury or death from fire and burn hazards. The recalled pig and toilet lighters violate the mandatory standard for cigarette lighters because they do not have the required child-resistant mechanisms, posing a serious risk of injury or death from fire and burn hazards.
- 2026-02-26CPSCRoyal Oak Enterprises, LLC, dba Royal Oak of Roswell, GeorgiaRoyal Oak Enterprises Recalls Lighters Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Violates Mandatory Standard for Multipurpose Lighters
The recalled lighters violate the mandatory standard for multipurpose lighters because they do not have the required child-resistant mechanisms, posing a risk of serious injury or death from fire and burn hazards. The lighters also violate the labeling requirements under the Federal Hazardous Substances Act by missing required safety information.
- 2026-02-26CPSCDupray USA LLC, of Newark, DelawareDupray USA Recalls Neat Steam Cleaners Due to Risk of Burn Hazards or Serious Injury
The steam cleaner's boiler can rupture if it is overfilled, corroded and the pressure release valve malfunctions, posing risk of burn hazards or serious injury to users or bystanders.
- 2026-02-26CPSCJiangsu Ever-Tie Lighting Co., Ltd, of ChinaPQL Recalls High Bay Linear LED Light Fixtures Due to Fire Hazard
The retaining pins used to secure the LED board inside some units can degrade, the LED board to come loose inside the fixture, posing a fire hazard.
- 2026-02-26CPSCSanven Technology Ltd., dba Vevor, of Rancho Cucamonga, CaliforniaSanven Technology Recalls Vevor Baby Gates Due to Risk of Serious Injury from Entrapment Hazard; Violates Mandatory Standard for Gates and Enclosures
The recalled gates violate the mandatory standard for expansion gates and expandable enclosures because a child's torso can fit through the opening between the gate and the floor, posing a risk of serious injury due to entrapment.
- 2026-02-25FDA-DeviceIntuitive Surgical, Inc.Class IIDa Vinci 5 ASSY, DV5 CONSOLE, IS5000 Model/Catalog Number: 380730 Used for minimally invasive surgery.
An error event following the release of a software version for the surgical system that can result in loss of user interface content on an external monitor or tower monitor.
- 2026-02-25FDA-DeviceStryker CorporationClass IIMOLLI 2 System System includes: MM1000 (Pack of 10) - MOLLI Introducer (8cm, 14G) and MOLLI Marker UDI (GTIN): 00850024195028 MS-00009 (Pack of 10) - MOLLI Introducer (12cm, 14G) and MOLLI Marker UDI (GTIN): 00850024195134 MP2001 - MOLLI 2 Wand UDI (GTIN): 00850024195141 MP2015A - MOLLI OncoPen UDI (GTIN): 00850024195219 MT2001 - MOLLI 2 Tablet UDI (GTIN): 00850024195158 The MOLLI Marker is intended to be placed percutaneously in soft tissue to temporarily mark a surgical s
Due to a need to update the product labeling (Instructions for Use IFU) as a result of the magnetized surgical tools dislodging markers using during target tissue removal procedures.
- 2026-02-25FDA-DeviceCentinel Spine, Inc.Class IIBrand Name: Prodisc Product Name: Prodisc C SK Model/Catalog Number: PDSL6 Software Version: N/A Product Description: Total cervical disc replacement Component: No
Products were mislabeled as the 6mm product but included the 5 mm product.
- 2026-02-25FDA-DeviceMedline Industries, LPClass IIMedline Surgical Packs: 1) PACK,UNIVERSAL,ULTRAGARD,5/CS, Model Number: DYNJP1050UG; 2) PACK,SHOULDER,DRAPE,POUCH,10/CSModel Number: DYNJP8401
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
- 2026-02-25FDA-DeviceMedline Industries, LPClass IIMedline Surgical Gowns: 1) GOWN,NONRNF,L,30/CS, Model Number: DYNJP2001; 2) GOWN,SIRUS,NONRNF,SETINSLV,L,20/CS, Model Number: DYNJP2001S; 3) GOWN,ECLIPSE,NONRNF,XL,ST,30/CS, Model Number: DYNJP2002; 4) GOWN,SIRUS,NONRNF,SETINSLV,XL,20/CS, Model Number: DYNJP2002S; 5) GOWN,SIRUS,NONRNF,XLN/XL,20/CS, Model Number: DYNJP2002SL; 6) GOWN,NONRNF,2XL,18/CS, Model Number: DYNJP2003; 7) GOWN,SIRUS,NONRNF,SETINSLV,2XL,18/CS, Model Number: DYNJP2003S; 8) GOWN,SIRUS,NONRNF,XLN/2XL,18/CS, Mode
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
- 2026-02-25FDA-DeviceMedline Industries, LPClass IIMedline Surgical Drapes: 1) SHEET,DRAPE,40X58,STERILE, Model Number: DYNJP2410; 2) DRAPE,SHEET,ECONOMY,40X58",ST,20/CS, Model Number: DYNJP2411; 3) SHEET,DRAPE, 40X70,STERILE, Model Number: DYNJP2412; 4) DRAPE,MEDIUM,TAPE,40X70",ST,50/CS, Model Number: DYNJP2412T; 5) SHEET,DRAPE,53X77,STERILE, Model Number: DYNJP2414; 6) DRAPE,SHEET,3/4,53X77",ST,20/CS, Model Number: DYNJP2414R; 7) DRAPE,SHEET,ULTRAGARD,20/CS, Model Number: DYNJP2414UG; 8) DRAPE,RNF,53X77",ST,20/CS, Model Number:
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
- 2026-02-25FDA-DeviceMedline Industries, LPClass IIMedline Convenience Kits: 1) ARTHROSCOPY CDS, Model Number: CDS984609B; 2) ARTHROSCOPY TRAYS, Model Number: DYNJ22501G; 3) ARTHROSCOPY PACK, Model Number: DYNJ32715F; 4) CHS ARTHROSCOPY PACK, Model Number: DYNJ50834C; 5) ARTHROSCOPY TRAY-LF, Model Number: DYNJ51069
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
- 2026-02-25FDA-DeviceMedline Industries, LPClass IIMedline Convenience Kits: 1) SPINAL CDS, Model Number: CDS940087AG; 2) SPINAL CDS, Model Number: CDS940087AI; 3) TOTAL HIP CDS-LF, Model Number: CDS980832Q; 4) TOTAL HIP CDS-LF, Model Number: CDS980832R; 5) TOTAL HIP CDS-LF, Model Number: CDS980832S; 6) TOTAL KNEE CDS-LF, Model Number: CDS980833Q; 7) TOTAL KNEE CDS-LF, Model Number: CDS980833R; 8) TOTAL HIP PROCEDURE, Model Number: CDS980865V; 9) TOTAL HIP PROCEDURE, Model Number: CDS980865W; 10) TOTAL HIP PROCEDURE, Model Num
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
- 2026-02-25FDA-DeviceMedline Industries, LPClass IIMedline Convenience Kits: 1) KIT OPHTHALMIC RUPTURE GLOBE, Model Number: DYKMBNDL104; 2) KIT OPHTHALMIC RUPTURE GLOBE, Model Number: DYKMBNDL104A; 3) KIT OPHTHALMOLOGY CORNEAL TRAN, Model Number: DYKMBNDL159; 4) KIT OPHTHALMOLOGY CATARACT, Model Number: DYKMBNDL180; 5) KIT OPHTHALMOLOGY EYE MUSCLE, Model Number: DYKMBNDL42; 6) KIT SURG ONC PORT INSERTION, Model Number: DYKMBNDL43B; 7) KIT SURG ONC EXCISION BREAST, Model Number: DYKMBNDL84B; 8) KIT OPTHAMOLOGY BASIC, Model Number:
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
- 2026-02-25FDA-DeviceMedline Industries, LPClass IIMedline Convenience Kits: 1) BAP NORTH ROBOTIC SURGERY CDS, Model Number: CDS982407N; 2) TOT/ GYN LITHOTOMY CDS, Model Number: CDS985431K; 3) TOT/ GYN LITHOTOMY CDS, Model Number: CDS985431O; 4) KIT ROBOTICS GYN, Model Number: DYKMBNDL109A; 5) KIT ROBOTICS UROLOGY PROSTATE, Model Number: DYKMBNDL116A; 6) KIT ROBOTICS UROLOGY PROSTATE, Model Number: DYKMBNDL116G; 7) ROBOTIC PACK, Model Number: DYNJ04135B; 8) MINOR LITHOTOMY PACK, Model Number: DYNJ04382J; 9) NBMC D & C PACK-LF, M
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
- 2026-02-25FDA-DeviceMedline Industries, LPClass IIMedline Convenience Kits: 1) HYSTEROSCOPY, Model Number: CDS984086I; 2) KIT GYN ONCOLOGY LAP, Model Number: DYKMBNDL91A; 3) VAGINAL HYSTERECTOMY PACK-LF, Model Number: DYNJ0373807J; 4) VAGINAL HYSTERECTOMY PACK-LF, Model Number: DYNJ0373807K; 5) MINOR VAGINAL #76-RF, Model Number: DYNJ27434R; 6) VAG HYST PACK, Model Number: DYNJ31344J; 7) VAG HYST PACK, Model Number: DYNJ31344K; 8) RRMC VAGINAL HYSTERECTOMY PACK, Model Number: DYNJ33393L; 9) RRMC VAGINAL HYSTERECTOMY PACK, Model
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
- 2026-02-25FDA-DeviceMedline Industries, LPClass IIMedline Convenience Kits: 1) C-SECTION PACK, Model Number: CDS820080N; 2) C-SECTION CDS, Model Number: CDS983523G; 3) C-SECTION, Model Number: CDSCCR611O; 4) C-SECTION, Model Number: CDSCCR611P; 5) LUD C-SECTION-LF, Model Number: DYNJ0101616I; 6) C-SECTION TRAY, Model Number: DYNJ15494G; 7) C-SECTION TRAY-LF, Model Number: DYNJ19529P; 8) C-SECTION TRAY-LF, Model Number: DYNJ19529Q; 9) C-SECTION TRAY-LF, Model Number: DYNJ19529R; 10) C-SECTION TRAY-LF, Model Number: DYNJ19529S;
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.